Association between RANTES polymorphisms and asthma severity among Tunisian children

被引:24
作者
Lachheb, Jihene [1 ]
Chelbi, Hanene
Hamzaoui, Kamel
Hamzaoui, Agnes
机构
[1] Med Univ Tunis, Homeostasis & Cell Dysfunct Unit Res 99 UR 08 40, Tunis, Tunisia
[2] Pneumol Hosp A Mami, Dept Pediat & Resp Dis, Ariana, Tunisia
关键词
asthma; RANTES; Polymorphisms; severity; allergy;
D O I
10.1016/j.humimm.2007.04.004
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 [免疫学];
摘要
The chemokine known as RANTES (regulated upon activation, normal T cells expressed and secreted) is an important element for the chemotaxis at the site of allergic inflammation. Many studies have made an interesting link between RANTES polymorphisms and asthma, showing that the variant in the promoter region is associated with high risk of asthma and severe airway obstruction. We conducted a case-control and family study aiming at identifying the relationship between polymorphisms (-28 C/G and -403 G/A) and haplotypes in the RANTES gene with asthma and severity. The results of the case control study suggest an association between alleles level of -28 C/G and -403 G/A promoter polymorphism (p = 0.01) (p = 0.00175) and asthma. Univariate analysis of the RANTES polymorphisms show an increased prevalence of the AC and AG haplotypes in asthmatics (p = 0.014) and (p = 0.015) respectively. Our data suggest that -28 C/G and -403 G/A polymorphisms within the RANTES promoter region play an important rote in asthma predisposition and in the severity of airway obstruction. (c) 2007 American Society for Histocompatibility and Immunogenetics. Published by Elsevier Inc. All rights reserved.
引用
收藏
页码:675 / 680
页数:6
相关论文
共 25 条
[1]
Preferential transmission and association of the -403 G→A promoter RANTES polymorphism with atopic asthma [J].
Al-Abdulhadi, SA ;
Helms, PJ ;
Main, M ;
Smith, O ;
Christie, G .
GENES AND IMMUNITY, 2005, 6 (01) :24-30
[2]
ALAM R, 1993, J IMMUNOL, V150, P3442
[3]
Increased MCP-1, RANTES, and MIP-1 alpha in bronchoalveolar lavage fluid of allergic asthmatic patients [J].
Alam, R ;
York, J ;
Boyars, M ;
Stafford, S ;
Grant, JA ;
Lee, J ;
Forsythe, P ;
Sim, T ;
Ida, N .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 1996, 153 (04) :1398-1404
[4]
The distribution of eosinophils and lymphocytes in the large and small airways of asthmatics [J].
Carroll, N ;
Cooke, C ;
James, A .
EUROPEAN RESPIRATORY JOURNAL, 1997, 10 (02) :292-300
[5]
Genome screen for asthma and related phenotypes in the French EGEA study [J].
Dizier, MH ;
Besse-Schmittler, C ;
Guilloud-Bataille, M ;
Annesi-Maesano, I ;
Boussaha, M ;
Bousquet, J ;
Charpin, D ;
Degioanni, A ;
Gormand, F ;
Grimfeld, A ;
Hochez, J ;
Hyne, G ;
Lockhart, A ;
Luillier-Lacombe, M ;
Matran, R ;
Meunier, F ;
Neukirch, F ;
Pacheco, Y ;
Parent, V ;
Paty, E ;
Pin, I ;
Pison, C ;
Scheinmann, P ;
Thobie, N ;
Vervloet, D ;
Kauffmann, F ;
Feingold, J ;
Lathrop, M ;
Demenais, F .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2000, 162 (05) :1812-1818
[6]
LOCALIZATION OF A HUMAN T-CELL-SPECIFIC GENE, RANTES (D17S136E), TO CHROMOSOME 17Q11.2-Q12 [J].
DONLON, TA ;
KRENSKY, AM ;
WALLACE, MR ;
COLLINS, FS ;
LOVETT, M ;
CLAYBERGER, C .
GENOMICS, 1990, 6 (03) :548-553
[7]
The-403 G→A promoter polymorphism in the RANTES gene is associated with atopy and asthma [J].
Fryer, AA ;
Spiteri, MA ;
Bianco, A ;
Hepple, M ;
Jones, PW ;
Strange, RC ;
Makki, R ;
Tavernier, G ;
Smilie, FI ;
Custovic, A ;
Woodcock, AA ;
Ollier, WER ;
Hajeer, AH .
GENES AND IMMUNITY, 2000, 1 (08) :509-514
[8]
A polymorphism at position-403 in the human RANTES promoter [J].
Hajeer, AH ;
Al Sharif, F ;
Ollier, WER .
EUROPEAN JOURNAL OF IMMUNOGENETICS, 1999, 26 (05) :375-376
[9]
A functional polymorphism in the RANTES gene promoter is associated with the development of late-onset asthma [J].
Hizawa, N ;
Yamaguchi, E ;
Konno, S ;
Tanino, Y ;
Jinushi, E ;
Nishimura, M .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2002, 166 (05) :686-690
[10]
RANTES and macrophage inflammatory protein 1 alpha selectively enhance immunoglobulin (IgE) and IgG4 production by human B cells [J].
Kimata, H ;
Yoshida, A ;
Ishioka, C ;
Fujimoto, M ;
Lindley, I ;
Furusho, K .
JOURNAL OF EXPERIMENTAL MEDICINE, 1996, 183 (05) :2397-2402